UPDATED: GlaxoSmithKline Recalling Ventolin Inhalers for Possible Package Leakage Asthma and Allergy Foundation of America

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A spokesperson for GlaxoSmithKline told Reuters at the time that the recall did not represent a risk to the public, and that the public were not required to return any affected inhalers. The voluntary recall targets Ventolin HFA Inhalation Aerosol, distributed via prescription nationwide. It is important to stay up-to-date on news about asthma and allergies. By joining our community and following our blog, you will be able to receive breaking news about research and treatments. Our community also provides an opportunity to connect with other patients who manage these conditions for peer support. The Asthma and Allergy Foundation of America is a non-profit organization and we are reporting this recall to inform people with asthma who rely on this medication.

Ventolin inhalers are used to treat a number of conditions, but are primarily prescribed as a treatment for asthma. Reuters reports the company saw a spike in complaints from customers about bulging on the outside wrapper of the inhalers, which indicates the propellant that delivers the medicine is leaking. GlaxoSmithKline is now looking into what may have caused the problem. GlaxoSmithKline is recalling nearly 600,000 Ventolin asthma inhalers in the United States because of a defect that may cause them to leak.

On 21 February 2018, the company announced a separate recall of certain lots of the Ventolin Accuhaler in the U.K. Once again, the cause was a manufacturing problem which led to "a small number of units not delivering the full number of doses," according to the U.K. Prices displayed on Our Platform are outside of Our control and may vary at any time. We provide no warranty regarding the accuracy, availability, or applicability of any of the pricing data or other information on Our Platform. The pricing estimates given are based on the most recent information available and may have changed when the prescription is filled at the pharmacy.

When functioning properly, the metered-dose inhaler releases a fixed dose of medication in aerosol form. GSK says patients using the inhalers are not in danger, so they don't need to return the product. People with inhalers that match the expiration date on the Ventolin HFA inhaler, but not the lot number, are not impacted by the recall. The following month, the company expanded the recall, including additional batches of the Ventolin HFA inhaler, the Asthma and Allergy Foundation of America reported. Viral Facebook posts have rehashed an old recall, causing hundreds of thousands of people unnecessary concern.

If you are interested in trying one of them, I would talk to your doctor to discuss what would be appropriate for you. Biotechs raised just $2.2 billion in new stock offerings this year, a decline of more than 80% from the roughly $14.7 billion drugmakers hauled in a year ago. "We currently don't anticipate a supply impact to Ventolin HFA 200D inhaler as a result of this issue," GSK added in a statement. “We currently don’t anticipate a supply impact to Ventolin HFA 200D inhaler as a result of this issue,” GSK said in a statement. Good Housekeeping participates in various affiliate marketing programs, which means we may get paid commissions on editorially chosen products purchased through our links to retailer sites.

– More than 593,000 asthma inhalers in the United States have been recalled because of a problem that could cause them to deliver less medication than intended. No other lots are affected by the voluntary recall, meaning that, regardless of expiration date or doses indicated in dose counters, only inhalers in these two lots are affected. A GSK spokesman spoke with AAFA and said the recall is due to some complaints about the overwrap, or pouches containing the inhalers, becoming inflated by leaking from the product. The leaking may cause the inhaler to deliver fewer doses than shown on the dose counter. Glaxo's Ventolin inhalers have been available since 1969, and are used by many of the 25 million asthmatics in the U.S.

If you need to fill a prescription for Ventolin HFA 200D, the voluntary recall should not affect pharmacy supplies. RxSpark is an easy-to-use pharmacy discount platform offering huge savings of up to 90% off prescriptions. Compare prices at pharmacies near you to find the best price and ensure you aren’t overpaying for your meds.

GlaxoSmithKline is voluntarily recalling Ventolin HFA Inhalation Aerosol 90 mcg per actuation, 200 Metered inhalations. A check of the web sites of the Food and Drug Administration and GlaxoSmithKline showed there was no new Ventolin inhaler recall in February 2018. When you block a person, they can no longer invite you to a private message or post to your profile wall. Replies and comments they make will be collapsed/hidden by default.

The recall only affects the U.S. market and does not extend to patients. The defect does not pose an immediate danger to patients, though it could cause the inhaler to deliver a lower dose of the medicine than specified on the package. Users are asked to return any inhalers they have already purchased. The FDA says a level II recall means use of the device "may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote." Drugmaker GSK recalling nearly 600,000 asthma inhalers in U.S. In April 2017, GlaxoSmithKline announced they were recalling almost 600,000 Ventolin HFA inhalers because a propellant leakage in the inhalers had caused them to emit a lower dosage of the medication albuterol.